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TIOCONAZOLE
TIOCONAZOLE - 63094-0426-1 - (TIOCONAZOLE)
Drug Information of TIOCONAZOLE
| Product NDC: | 63094-0426 |
| Proprietary Name: | TIOCONAZOLE |
| Non Proprietary Name: | TIOCONAZOLE |
| Active Ingredient(s): | 65 mg/g & nbsp; TIOCONAZOLE |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TIOCONAZOLE
| Product NDC: | 63094-0426 |
| Labeler Name: | DPT Laboratories, Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075915 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070822 |
Package Information of TIOCONAZOLE
| Package NDC: | 63094-0426-1 |
| Package Description: | 5 g in 1 APPLICATOR (63094-0426-1) |
NDC Information of TIOCONAZOLE
| NDC Code | 63094-0426-1 |
| Proprietary Name | TIOCONAZOLE |
| Package Description | 5 g in 1 APPLICATOR (63094-0426-1) |
| Product NDC | 63094-0426 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TIOCONAZOLE |
| Dosage Form Name | OINTMENT |
| Route Name | VAGINAL |
| Start Marketing Date | 20070822 |
| Marketing Category Name | ANDA |
| Labeler Name | DPT Laboratories, Ltd. |
| Substance Name | TIOCONAZOLE |
| Strength Number | 65 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
